Transcription of Harmonised Technical Guidance for Non-eCTD electronic ...
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Technical NeeS Guidance Page 1 of 19 Guidance for Industry on Providing Regulatory Information in electronic Format Harmonised Technical Guidance for Non-eCTD electronic Submissions (NeeS) for human medicinal products in the EU Version October 2013 Technical NeeS Guidance Page 2 of 19 Table of Content 1 Introduction .. 32 General considerations .. Scope .. Types of product Types of submission Types of procedures Exceptions Structure of submissions .. Dossier Structure Table of Contents and bookmarks Moving to NeeS format applications .. General Submission Considerations.
Technical NeeS Guidance v4.0 Page 1 of 19. Guidance for Industry on Providing Regulatory Information in Electronic Format . Harmonised Technical Guidance for
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CONFORMITY ASSESSMENT IN EU TECHNICAL, Conformity assessment in eu technical harmonisation, Safety Risk Assessment of Infrared Emitting, Technical, Conformity Assessment of Medical Devices Under, Conformity Assessment of. Medical Devices Under, Conformity Risk Assessment To Comply, Recreational Craft Directive 2013/53, Conformity, PERSONAL PROTECTIVE EQUIPMENT DIRECTIVE (, Personal Protective Equipment Directive 89, December 2012 RoHS 2 FAQ, European Commission, December 2012, RoHS 2 FAQ, DIRECTIVE 2011/65/EU, HazLoc Essential Guides, Intertek